Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Cristina Ciancimino"'
Autor:
Barbara Parrino, Anna Carbone, Gloria Di Vita, Cristina Ciancimino, Alessandro Attanzio, Virginia Spanò, Alessandra Montalbano, Paola Barraja, Luisa Tesoriere, Maria Antonia Livrea, Patrizia Diana, Girolamo Cirrincione
Publikováno v:
Marine Drugs, Vol 13, Iss 4, Pp 1901-1924 (2015)
A new series of nortopsentin analogues, in which the imidazole ring of the natural product was replaced by thiazole and the indole unit bound to position 2 of the thiazole ring was substituted by a 7-azaindole moiety, was efficiently synthesized. Two
Externí odkaz:
https://doaj.org/article/8d75a9ae9c604ffd94446f6f7c2fe963
Synthesis of substituted isoindolo[2,1-a]quinoxalin-6-yl–amino and 6-imino-5-yl thiourea derivatives
Autor:
Barbara Parrino, Cristina Ciancimino, Chandrakant Sarwade, Virginia Spanò, Alessandra Montalbano, Paola Barraja, Girolamo Cirrincione, Patrizia Diana, Anna Carbone
Publikováno v:
ARKIVOC, Vol 2014, Iss 5, Pp 384-398 (2014)
Externí odkaz:
https://doaj.org/article/7aeb702456364ecf9cbedcf297220f46
Autor:
Gianfranco Favi, Cristina Ciancimino, Barbara Parrino, Orazio A. Attanasi, Virginia Spanò, Anna Carbone
Publikováno v:
Molecules, Vol 18, Iss 3, Pp 2518-2527 (2013)
A series of substituted ethyl 1-[(tert-butoxycarbonyl)amino]-2-methyl-5- (1-methyl-1H-indol-3-yl)-4-[(1-methyl-1H-indol-3-yl)carbonyl]-1H-pyrrole-3-carboxylates were prepared in excellent yields (82-98%) by one-pot reactions between β-dicarbonyl com
Externí odkaz:
https://doaj.org/article/90999f6393c8488e8cf8098e2e000a10
Publikováno v:
ARKIVOC, Vol 2012, Iss 2, Pp 41-49 (2012)
Externí odkaz:
https://doaj.org/article/b3a6111e97904d80ba313031dcc87cb5
Synthesis of substituted isoindolo[2,1-a]quinoxalin-6-yl–amino and 6-imino-5-yl thiourea derivatives
Autor:
Anna Carbone, Virginia Spanò, Girolamo Cirrincione, Barbara Parrino, Patrizia Diana, Cristina Ciancimino, Chandrakant Sarwade, Alessandra Montalbano, Spanò, Paola Barraja
Publikováno v:
ARKIVOC, Vol 2014, Iss 5, Pp 384-398 (2014)
A series of substituted 1-(5-bromopyridin-2-yl)-3-[2-(isoindolo[2,1-a]quinoxalin-6- ylamino)ethyl]thiourea and 1-(5-bromopyridin-2-yl)-3-[2-(6-iminoisoindolo[2,1-a]quinoxalin- 5(6H)-yl)ethyl]thiourea derivatives were prepared in good yields (63-85%)
Autor:
Alessandra Montalbano, Patrizia Diana, Anna Carbone, Barbara Parrino, Paola Barraja, Virginia Spanò, Cristina Ciancimino, Girolamo Cirrincione
Publikováno v:
ChemInform. 47
Two new ring systems, isoindolo[1,4]benzoxazinone and isoindolo[1,5]benzoxazepine, were conveniently synthesized through cyclization of suitably substituted isoindole derivatives. Some of the new compounds exhibited antiproliferative activity against
Autor:
Patrizia Diana, Gloria Di Vita, Girolamo Cirrincione, M. A. Livrea, Anna Carbone, Cristina Ciancimino, Luisa Tesoriere, Paola Barraja, Alessandro Attanzio, Virginia Spanò, Barbara Parrino, Alessandra Montalbano
Publikováno v:
Marine Drugs, Vol 13, Iss 4, Pp 1901-1924 (2015)
Marine Drugs
Volume 13
Issue 4
Pages 1901-1924
Marine Drugs
Volume 13
Issue 4
Pages 1901-1924
A new series of nortopsentin analogues, in which the imidazole ring of the natural product was replaced by thiazole and the indole unit bound to position 2 of the thiazole ring was substituted by a 7-azaindole moiety, was efficiently synthesized. Two
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7471c818fd2a702c95de33aa51e7eef6
http://hdl.handle.net/10447/145699
http://hdl.handle.net/10447/145699
Autor:
Claudia Sissi, Paola Barraja, Patrizia Diana, Marzia Pennati, Odra Pinato, Girolamo Cirrincione, Virginia Spanò, Cristina Ciancimino, Manlio Palumbo, Barbara Parrino, Nadia Zaffaroni, Alessandra Montalbano, Péter Mátyus, Marco Folini, Anna Carbone, Giovanni Luca Beretta, Balázs Balogh
Water-soluble isoindoloquinoxalin (IIQ) imines and the corresponding acetates were conveniently prepared from the key intermediates 2-(2′-aminophenyl)-2H-isoindole-1-carbonitriles obtained by a Strecker reaction between substituted 1,2-dicarbaldehy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::42dab2037edb235d0cd47236c862ff80
http://hdl.handle.net/11577/3182352
http://hdl.handle.net/11577/3182352
Autor:
Giulia Vignaroli, Stephan A. Ohnmacht, Mekala Gunaratnam, Stephen Neidle, Cristina Ciancimino
Using a phenotypic screening and SAR optimization approach, a phenyl-bis-oxazole derivative has been identified with anti-proliferative activity, optimized with the use of a panel of cancer cell lines. The lead compound was synthesized by means of a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15e96ba847598c5f1e1ec1e1da6f0d0f
http://hdl.handle.net/10447/85543
http://hdl.handle.net/10447/85543
Autor:
Carbone, Anna1 anna.carbone@unipa.it, Spanò, Virginia1, Parrino, Barbara1, Ciancimino, Cristina1, Attanasi, Orazio A.2, Favi, Gianfranco2 gianfranco.favi@uniurb.it
Publikováno v:
Molecules. Mar2013, Vol. 18 Issue 3, p2518-2527. 10p. 3 Diagrams.